Xu Weili, Wong Glenn, Hwang You Yi, Larbi Anis
Singapore Immunology Network (SIgN), Agency for Science Technology and Research (A*STAR), Immunos, Singapore, Singapore.
Department of Geriatrics, Faculty of Medicine, University of Sherbrooke, Sherbrooke, QC, J1K 2R1, Canada.
Semin Immunopathol. 2020 Oct;42(5):559-572. doi: 10.1007/s00281-020-00824-x. Epub 2020 Nov 9.
From a holistic point of view, aging results from the cumulative erosion of the various systems. Among these, the immune system is interconnected to the rest as immune cells are present in all organs and recirculate through bloodstream. Immunosenescence is the term used to define the remodelling of immune changes during aging. Because immune cells-and particularly lymphocytes-can further differentiate after their maturation in response to pathogen recognition, it is therefore unclear when senescence is induced in these cells. Additionally, it is also unclear which signals triggers senescence in immune cells (i) aging per se, (ii) specific response to pathogens, (iii) underlying conditions, or (iv) inflammaging. In this review, we will cover the current knowledge and concepts linked to immunosenescence and we focus this review on lymphocytes and T cells, which represent the typical model for replicative senescence. With the evidence presented, we propose to disentangle the senescence of immune cells from chronological aging.
从整体观点来看,衰老源于各种系统的累积性损耗。其中,免疫系统与其他系统相互关联,因为免疫细胞存在于所有器官中,并通过血液循环进行再循环。免疫衰老这一术语用于定义衰老过程中免疫变化的重塑。由于免疫细胞——尤其是淋巴细胞——在成熟后可因病原体识别而进一步分化,因此尚不清楚这些细胞何时会诱导衰老。此外,也不清楚是哪些信号触发免疫细胞衰老:(i)衰老本身,(ii)对病原体的特异性反应,(iii)潜在病症,还是(iv)炎症衰老。在本综述中,我们将涵盖与免疫衰老相关的当前知识和概念,并将本综述聚焦于淋巴细胞和T细胞,它们代表了复制性衰老的典型模型。基于所提供的证据,我们建议将免疫细胞衰老与自然衰老区分开来。